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iTEAR100 Therapy for Dry Eye Syndrome

Phase 4
Waitlist Available
Research Sponsored by Olympic Ophthalmics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Inclusion Criteria: Able to sign English language consent form and over age 18 and reside in the U.S.
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Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 days
Awards & highlights

Study Summary

A Usability Study of External Neuromodulation With iTEAR100 Generation 2. A study which evaluates user ability to train and access the iTEAR100 device in a telehealth environment.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and 30 days for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Usability
Secondary outcome measures
Adverse Events
Symptom Score
Symptom Scores

Trial Design

1Treatment groups
Experimental Treatment
Group I: iTEAR100 TherapyExperimental Treatment1 Intervention
Treatment Arm. Assessment of usability of generation 2 connected devices

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Who is running the clinical trial?

Olympic Ophthalmics, Inc.Lead Sponsor
3 Previous Clinical Trials
265 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
A Usability Study of External Neuromodulation With iTEAR100 Generation 2
2022. "A Usability Study of External Neuromodulation With iTEAR100 Generation 2". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05304650.
~32 spots leftby May 2025
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